Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C1848029
Disease: Ehlers-Danlos syndrome caused by tenascin-X deficiency
Ehlers-Danlos syndrome caused by tenascin-X deficiency 		2 0 2 0.67 0 0
CUI: C0007871
Disease: Uterine Cervical Incompetence
Uterine Cervical Incompetence 		1 0 1 0.33 0 0
CUI: C0238590
Disease: Acrogeria
Acrogeria 		1 0 1 0.33 0 0
CUI: C0268288
Disease: Mild steroid 21-hydroxylase deficiency
Mild steroid 21-hydroxylase deficiency 		1 0 1 0.33 0 0
CUI: C0340649
Disease: Dissection of iliac artery
Dissection of iliac artery 		1 0 1 0.33 0 0
CUI: C0345002
Disease: Quadricuspid aortic valve
Quadricuspid aortic valve 		1 0 1 0.33 0 0
CUI: C0406584
Disease: Acrogeria, gottron type
Acrogeria, gottron type 		1 0 1 0.33 0 0
CUI: C1390214
Disease: Internal hemorrhage
Internal hemorrhage 		1 0 1 0.33 0 0
CUI: C1851811
Disease: Hypermobility of distal interphalangeal joints
Hypermobility of distal interphalangeal joints 		1 0 1 0.33 0 0
CUI: C1853365
Disease: AORTIC ANEURYSM, FAMILIAL ABDOMINAL 1
AORTIC ANEURYSM, FAMILIAL ABDOMINAL 1 		1 0 1 0.33 0 0
CUI: C1859995
Disease: Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency
Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency 		1 0 1 0.33 0 0
CUI: C1859998
Disease: CARCINOMA, ADRENOCORTICAL, ANDROGEN-SECRETING
CARCINOMA, ADRENOCORTICAL, ANDROGEN-SECRETING 		1 0 1 0.33 0 0
CUI: C3151153
Disease: ADENOMA, CORTISOL-PRODUCING
ADENOMA, CORTISOL-PRODUCING 		1 0 1 0.33 0 0
CUI: C3838669
Disease: Simple Virilizing 21-Hydroxylase Deficiency
Simple Virilizing 21-Hydroxylase Deficiency 		1 0 1 0.33 0 0
CUI: C4014831
Disease: VESICOURETERAL REFLUX 8
VESICOURETERAL REFLUX 8 		1 0 1 0.33 0 0
CUI: C4540530
Disease: EHLERS-DANLOS SYNDROME, NONVASCULAR VARIANT
EHLERS-DANLOS SYNDROME, NONVASCULAR VARIANT 		1 0 1 0.33 0 0
CUI: C4693985
Disease: EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 1
EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 1 		1 0 1 0.33 0 0
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV 		7 391 2 0.25 1 2.5E-03
CUI: C0342464
Disease: Salt-losing congenital adrenal hyperplasia
Salt-losing congenital adrenal hyperplasia 		2 0 1 0.25 0 0
CUI: C0406481
Disease: Comedonal acne
Comedonal acne 		2 0 1 0.25 0 0
CUI: C0426317
Disease: Genitourinary symptoms
Genitourinary symptoms 		2 0 1 0.25 0 0
CUI: C0524948
Disease: Maxillofacial Abnormalities
Maxillofacial Abnormalities 		2 0 1 0.25 0 0
CUI: C1834819
Disease: MYXOMATOUS MITRAL VALVE PROLAPSE 1
MYXOMATOUS MITRAL VALVE PROLAPSE 1 		2 0 1 0.25 0 0
CUI: C1857693
Disease: Arteriovenous fistulas of celiac and mesenteric vessels
Arteriovenous fistulas of celiac and mesenteric vessels 		2 0 1 0.25 0 0
CUI: C2752038
Disease: HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 4
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 4 		2 0 1 0.25 0 0